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Drug company (FDA labeler)

Vitruvias Therapeutics

NDC labeler code: 69680

What is a labeler?

The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.

Official FDA data only

Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.

Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.

At a glance

11Products (NDC)

Prescription medicines

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
December 27, 2023ANDA213213 Aminocaproic acid
AMINOCAPROIC ACID
Sunny
January 4, 2019ANDA210339 Propafenone hydrochloride
PROPAFENONE HYDROCHLORIDE
Sinotherapeutics Inc
December 18, 2018ANDA209255 Cyanocobalamin
CYANOCOBALAMIN
H2-Pharma
November 27, 2018ANDA209060 Aminocaproic acid
AMINOCAPROIC ACID
Sunny
August 21, 2017ANDA208652 Bupropion
BUPROPION HYDROCHLORIDE
Sinotherapeutics Inc

The sponsor is the company that holds the FDA application; it can differ from the labeler.

Recall timeline

No recall of these products (by NDC code) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026

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